MCB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental materials
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ganot, P.
Right arrow Articles by Thompson, E. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ganot, P.
Right arrow Articles by Thompson, E. M.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, September 2004, p. 7795-7805, Vol. 24, No. 17
0270-7306/04/$08.00+0     DOI: 10.1128/MCB.24.17.7795-7805.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Spliced-Leader RNA trans Splicing in a Chordate, Oikopleura dioica, with a Compact Genome{dagger}

Philippe Ganot,1 Torben Kallesøe,1 Richard Reinhardt,2 Daniel Chourrout,1 and Eric M. Thompson1*

Sars International Centre for Marine Molecular Biology, Bergen High Technology Centre, Bergen, Norway,1 Max Planck Institute for Molecular Genetics, Berlin, Germany2

Received 5 May 2004/ Returned for modification 24 May 2004/ Accepted 7 June 2004

trans splicing of a spliced-leader RNA (SL RNA) to the 5' ends of mRNAs has been shown to have a limited and sporadic distribution among eukaryotes. Within metazoans, only nematodes are known to process polycistronic pre-mRNAs, produced from operon units of transcription, into mature monocistronic mRNAs via an SL RNA trans-splicing mechanism. Here we demonstrate that a chordate with a highly compact genome, Oikopleura dioica, now joins Caenorhabditis elegans in coupling trans splicing with processing of polycistronic transcipts. We identified a single SL RNA which associates with Sm proteins and has a trimethyl guanosine cap structure reminiscent of spliceosomal snRNPs. The same SL RNA, estimated to be trans-spliced to at least 25% of O. dioica mRNAs, is used for the processing of both isolated or first cistrons and downstream cistrons in a polycistronic precursor. Remarkably, intercistronic regions in O. dioica are far more reduced than those in either nematodes or kinetoplastids, implying minimal cis-regulatory elements for coupling of 3'-end formation and trans splicing.


* Corresponding author. Mailing address: Sars International Centre for Marine Molecular Biology, Bergen High Technology Centre, Thormøhlensgt. 55, N-5008 Bergen, Norway. Phone: 47-55.58.43.46. Fax: 47-55.58.43.05. E-mail: Eric.Thompson{at}sars.uib.no.

{dagger} Supplemental data for this article may be found at http://mcb.asm.org/.


Molecular and Cellular Biology, September 2004, p. 7795-7805, Vol. 24, No. 17
0022-538X/04/$08.00+0     DOI: 10.1128/MCB.24.17.7795-7805.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2004 by the American Society for Microbiology. All rights reserved.